NP-MRD: Showing NP-Card for 10-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-8-ethyl-1,6,11-trihydroxy-9,10-dihydrotetracene-5,12-dione (NP0272683)

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Record Information

Version

2.0

Created at

2022-09-08 19:24:14 UTC

Updated at

2022-09-08 19:24:14 UTC

NP-MRD ID

NP0272683

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-8-ethyl-1,6,11-trihydroxy-9,10-dihydrotetracene-5,12-dione

Description

7-[(4-Amino-5-hydroxy-6-methyloxan-2-yl)oxy]-9-ethyl-4,6,11-trihydroxy-5,7,8,12-tetrahydrotetracene-5,12-dione belongs to the class of organic compounds known as acylsalicylic acids. These are o-acylated derivatives of salicylic acid. 10-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-8-ethyl-1,6,11-trihydroxy-9,10-dihydrotetracene-5,12-dione is found in Nonomuraea roseoviolacea. 7-[(4-Amino-5-hydroxy-6-methyloxan-2-yl)oxy]-9-ethyl-4,6,11-trihydroxy-5,7,8,12-tetrahydrotetracene-5,12-dione is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241508342D          

 35 39  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004241508342D          

 35 39  0  0  0  0            999 V2000
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M  END
> <DATABASE_ID>
NP0272683

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC1=CC2=C(O)C3=C(C(O)=C2C(C1)OC1CC(N)C(O)C(C)O1)C(=O)C1=C(O)C=CC=C1C3=O

> <INCHI_IDENTIFIER>
InChI=1S/C26H27NO8/c1-3-11-7-13-19(16(8-11)35-17-9-14(27)22(29)10(2)34-17)26(33)21-20(24(13)31)23(30)12-5-4-6-15(28)18(12)25(21)32/h4-7,10,14,16-17,22,28-29,31,33H,3,8-9,27H2,1-2H3

> <INCHI_KEY>
KURBZXMNPPHYKQ-UHFFFAOYSA-N

> <FORMULA>
C26H27NO8

> <MOLECULAR_WEIGHT>
481.501

> <EXACT_MASS>
481.173666833

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
50.7245896124618

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-9-ethyl-4,6,11-trihydroxy-5,7,8,12-tetrahydrotetracene-5,12-dione

> <ALOGPS_LOGP>
2.13

> <JCHEM_LOGP>
3.5643901117354955

> <ALOGPS_LOGS>
-3.29

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
8.431924175308199

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.819979840956234

> <JCHEM_PKA_STRONGEST_BASIC>
9.37100620848962

> <JCHEM_POLAR_SURFACE_AREA>
159.54

> <JCHEM_REFRACTIVITY>
127.10739999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.48e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
10-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-8-ethyl-1,6,11-trihydroxy-9,10-dihydrotetracene-5,12-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.002  -3.080   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      10.669  -3.080   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.337  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.670  -5.390   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.670  -6.930   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.337  -7.700   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      13.337  -9.240   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.669  -7.700   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      10.669  -9.240   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       8.002  -9.240   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
HETATM   30  N   UNK     0       2.667 -13.860   0.000  0.00  0.00           N+0
HETATM   31  C   UNK     0       1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       0.000 -12.320   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       2.667  -9.240   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   25                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   23                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   20                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   11   18                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18    8   21                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21    5   24                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24    3                                                       
CONECT   26   24   27                                                       
CONECT   27   26   28   35                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   27                                                       
MASTER        0    0    0    0    0    0    0    0   35    0   78    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₂₇NO₈

Average Mass

481.5010 Da

Monoisotopic Mass

481.17367 Da

IUPAC Name

7-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-9-ethyl-4,6,11-trihydroxy-5,7,8,12-tetrahydrotetracene-5,12-dione

Traditional Name

10-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-8-ethyl-1,6,11-trihydroxy-9,10-dihydrotetracene-5,12-dione

CAS Registry Number

Not Available

SMILES

CCC1=CC2=C(O)C3=C(C(O)=C2C(C1)OC1CC(N)C(O)C(C)O1)C(=O)C1=C(O)C=CC=C1C3=O

InChI Identifier

InChI=1S/C26H27NO8/c1-3-11-7-13-19(16(8-11)35-17-9-14(27)22(29)10(2)34-17)26(33)21-20(24(13)31)23(30)12-5-4-6-15(28)18(12)25(21)32/h4-7,10,14,16-17,22,28-29,31,33H,3,8-9,27H2,1-2H3

InChI Key

KURBZXMNPPHYKQ-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Nonomuraea roseoviolacea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as acylsalicylic acids. These are o-acylated derivatives of salicylic acid.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Acylsalicylic acids

Alternative Parents

Substituents

Acylsalicylic acid
Phenol ester
Tricarboxylic acid or derivatives
Benzoic acid
Phenoxy compound
Benzoyl
Carboxylic acid ester
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	2.13	ALOGPS
logP	3.56	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	7.82	ChemAxon
pKa (Strongest Basic)	9.37	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	159.54 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	127.11 m³·mol⁻¹	ChemAxon
Polarizability	50.72 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

160308

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 10-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-8-ethyl-1,6,11-trihydroxy-9,10-dihydrotetracene-5,12-dione (NP0272683)

MOL for NP0272683 (10-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-8-ethyl-1,6,11-trihydroxy-9,10-dihydrotetracene-5,12-dione)

3D MOL for NP0272683 (10-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-8-ethyl-1,6,11-trihydroxy-9,10-dihydrotetracene-5,12-dione)

3D SDF for NP0272683 (10-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-8-ethyl-1,6,11-trihydroxy-9,10-dihydrotetracene-5,12-dione)

3D-SDF for NP0272683 (10-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-8-ethyl-1,6,11-trihydroxy-9,10-dihydrotetracene-5,12-dione)

PDB for NP0272683 (10-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-8-ethyl-1,6,11-trihydroxy-9,10-dihydrotetracene-5,12-dione)

3D PDB for NP0272683 (10-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-8-ethyl-1,6,11-trihydroxy-9,10-dihydrotetracene-5,12-dione)

SMILES for NP0272683 (10-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-8-ethyl-1,6,11-trihydroxy-9,10-dihydrotetracene-5,12-dione)

INCHI for NP0272683 (10-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-8-ethyl-1,6,11-trihydroxy-9,10-dihydrotetracene-5,12-dione)

Structure for NP0272683 (10-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-8-ethyl-1,6,11-trihydroxy-9,10-dihydrotetracene-5,12-dione)

3D Structure for NP0272683 (10-[(4-amino-5-hydroxy-6-methyloxan-2-yl)oxy]-8-ethyl-1,6,11-trihydroxy-9,10-dihydrotetracene-5,12-dione)